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1,4-Dibromobutane → 3-(4-Bromobutyl)bicyclo[4.2.0]octa-1(6),2,4-triene

HRID 42397
ノート
印刷プレビュー

反応式

HRID 42397 の反応式
Br[C:2]1[CH:9]=[CH:8][C:5]2[CH2:6][CH2:7][C:4]=2[CH:3]=1.C([Li])(C)(C)C.[Br:15][CH2:16][CH2:17][CH2:18][CH2:19]Br>>[Br:15][CH2:16][CH2:17][CH2:18][CH2:19][C:2]1[CH:9]=[CH:8][C:5]2[CH2:6][CH2:7][C:4]=2[CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 80561,4-DibromobutaneHCID 108669803-Bromobicyclo[4.2.0]octa-1,3,5-trieneHCID 178418306HCID 178418306、化合物

生成物 1

HCID 580284923-(4-Bromobutyl)bicyclo[4.2.0]octa-1(6),2,4-triene

反応条件

温度
-20 °C

実験手順

To a clean and dry 1000 ml round bottom flask equipped with a 250 ml addition funnel, low temperature thermometer and magnetic stir bar was transferred anhydrous tetrahydrofuran (500.0 ml) under nitrogen. 4-bromobenzocyclobutane (25.0 g, 0.1370 mol) was added to this flask by syringe. The reaction vessel was placed into a dry ice/acetone bath until a temperature of <−70° C. was achieved. The reaction mixture was then allowed to stir for 45 minutes at a stirring speed of 550 rpm in order to verify the integrity of the stirring apparatus at this temperature. Tert-butyllithium solution (161 ml, 0.2730 mol) was transferred to the addition funnel by cannula, then added dropwise to the reaction never allowing the temperature to rise above −65° C. Following addition, the reaction was allowed to stir for a period of 30 minutes. The vessel was then removed from the dry ice/acetone bath and allowed to warm to a temperature of −20° C. The vessel was then again placed into the dry ice/acetone bath until a temperature of <−70° was achieved. 1,4-dibromobutane (64.7 ml, 0.5460 mol) was added to the reaction dropwise via syringe, maintaining the current temperature. The reaction was allowed to stir for 30 minutes at this temperature following addition. The reaction was slowly warmed to room temperature over the following 12 hours. Reaction completion was confirmed by GC-MS. After warming, the reaction was quenched by the addition of isopropanol (25.0 ml) via syringe.

後処理

  1. customTo a clean and dry 1000 ml round bottom flask
  2. customequipped with a 250 ml addition funnel
  3. customThe reaction vessel was placed into a dry ice/acetone bath until a temperature of <−70° C.
  4. additionadded dropwise to the reaction
  5. customto rise above −65° C
  6. additionaddition
  7. stirringto stir for a period of 30 minutes
  8. customThe vessel was then removed from the dry ice/acetone bath
  9. customwas then again placed into the dry ice/acetone bath until a temperature of <−70°
  10. temperaturemaintaining the current temperature
  11. stirringto stir for 30 minutes at this temperature
  12. additionaddition
  13. temperatureThe reaction was slowly warmed to room temperature over the following 12 hours
  14. customReaction completion
  15. temperatureAfter warming
  16. customthe reaction was quenched by the addition of isopropanol (25.0 ml) via syringe

出典と根拠

ORDレコード
ord-0492a05c0b9143ad91432e2522b82560
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08535974B2

反応ノート

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